106689-40-1

Basic information

• Product Name: 2(1H)-Pyridinone,4-hydrazino-5-methyl-(9CI)
• Synonyms: 2(1H)-Pyridinone,4-hydrazino-5-methyl-(9CI)
• CAS NO: 106689-40-1
• Molecular Formula: C₆H₉N₃O
• Molecular Weight: 139.15516
• Product Categories: PYRIDINE
• Mol File: 106689-40-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 374.1°C at 760 mmHg
• Flash Point: 180.1°C
• Appearance: /
• Density: 1.24g/cm³
• Vapor Pressure: 8.53E-06mmHg at 25°C
• Refractive Index: 1.596
• CAS DataBase Reference: 2(1H)-Pyridinone,4-hydrazino-5-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Pyridinone,4-hydrazino-5-methyl-(9CI)(106689-40-1)
• EPA Substance Registry System: 2(1H)-Pyridinone,4-hydrazino-5-methyl-(9CI)(106689-40-1)

Safety Data

• Hazardous Substances Data: 106689-40-1(Hazardous Substances Data)

Usage

Structure

A pyridinone derivative with a hydrazino group (-NHNH2) and a methyl group (-CH3) attached to it

Type

A chemical compound

Potential applications

In pharmaceutical and medicinal chemistry as a precursor or intermediate in the synthesis of biologically active molecules

Further studies needed

To determine its specific properties and potential uses

InChI:InChI=1/C6H9N3O/c1-4-3-8-6(10)2-5(4)9-7/h2-3H,7H2,1H3,(H2,8,9,10)

Upstream product

• 41935-71-1 4-Hydroxy-5-methyl-2-oxo-1,2-dihydropyridine 

Relevant articles and documents

AUTRE VOIE D'ACCES AUX 5H-PYRIDOPYRROLOPYRIDINES ET LEUR TRANSFORMATION EN DERIVES N-5 ET N-8 SUBSTITUES

4-hydrazino-1H-pyridin-2-ones obtained starting from corresponding 2,4-dihydroxypiridines react with N-acetyl 4-piperidone.The expected hydrazones then give 6,7,8,9-tetrahydro 8-acetyl-2H,5H-pyridopyrrolopyridin-1-ones by thermal Fischer indole reaction.Aromatization of these last compounds with 10 percent palladized charchoal gives 2H,5H-pyridopyrrolopyridin-1-ones providing a new reaction pathway to this series which is more convenient that the one described in the preceding paper.Whereas the alkylation of the N-matallated species derived from 1-chloro-4-methyl-5H-pyridopyrrolopyridine by alkyl halides leads to the mixture of N-5 and N-8 alkyl derivatives, 1-chloro-5H-pyridopyrrolopyridine gives only the N-5 alkylated compound.